Tag | Content |
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EnhancerAtlas ID | HS187-05168 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:133797340-133799560 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr11:133797663-133797677 | CTGCCACGTCACCA | + | 7.42 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 133797860 | 133798306 | chr11 | 133798392 | 133798947 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I133927 | chr11 | 133797236 | 133799251 |
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Enhancer Sequence | GTATGGGGAT AAGCGGCTCA ACAGTGGCAG GATGAGGGAA GGAGCCCAGG ACCTGGCTGC 60 ACACACCCCC AGGGACAGCT GAAGTAGGGC CTCGGGTAAC CCACAGGGCT CATTCATCCA 120 ATCAGACTGG AGTCACCTGA GATGTCCAGG GTATAAGACC ATAATGACCA GGGGTTTCCC 180 CACAGTGGGG CCAGGATCCC TAAGGCCGTA AGGGTTGGAA GAAGGTCACG CTATGCATGG 240 AGAGTAGGAA GACGGGCCGA GGGTGTTCCC TTGTTCCACA GGCTCCCAAC TCCCAGCAAA 300 GCCGGAGGGC TATGGGTGCA GTGCTGCCAC GTCACCACAG GGAGGAGACA TGGTCCTGTG 360 GGACTGGCCC TCTCCTTGCA GCCCTGAGCT GTAACCTGGT GGGTGCCCTC CAGGATCCAC 420 TCCCGGGTCC CGGCTCACTA CCGTGCACGC CCAGGAGGGT GAGATGAGGC AGCGGAAAGC 480 AGTACAAAAA GAAGCCGGCG CCAAACGTCG GAGTCAGTGC ACAGAGTTAG AGGCAGGCAG 540 AAAGAAAGGA GACCTCCCCA ACCTCGGCCC CGCCCTTCCC TGGCCCAGGC AACAAAGCAG 600 CGAGGAGCCA CGTGTGGAAA AGCAGTGCAG ATGAGCAGCA GCGTGGAGCA GCAGCGTGAA 660 GCAGCACCGC AAGCAGCAGG GGAGCCCCAA TCTACACCTG AGCCCCCCAT CGTATGCCCA 720 GACCTCCCAC CCAGGCATCT CCAAAGACAG CTTGACCACA CCAAATGTCC CACCCTGGAC 780 ACCTAGGCGC TGAGCAGCAC CGGTCTCCCA GCAGCCACCG GGCAGGCTGG TTAGGGCCCC 840 CACGCTGCTG CGGGAGGAAC AGAGTAAGGG GACGGGAGGT GAGCTGCGGC AACTCCCATC 900 ATCCAGGTGC AGTTCTCCAA TCAGAATCAA GACACCCAGG ACACTCCGCC CGGGAAGCAG 960 CCACCGAACC ACCATGATGG GAGACAGAGC GGGTGCCCCT CTCAACTTCC CTCGCTGCTG 1020 AGAAGTGGAT AAAGGGGTCT CCCTGAACCC CCTGAGCTGC CCCAGGTGCC TGCCTTTTCC 1080 CCCTCCCCTC GAGCTCCCCC TCCTCGAGTT GAGCCTGGCT AGAGAGACAC CTGCAGGTGA 1140 GACAGGTCTA AAAGAAGGCA CTGAGGGGCT CGCCCTCCCA GCTCAAGGTT GTCACCCCCG 1200 GGGCAGGGCA GGTGGCTGCC ACTCTTACTC AAACAGGAGT GTAGGGAGGG GCAGCCCTTG 1260 GGGGTGGGAG GAGTCAGCTA GGCTTCCTTC TCCTCCCTTC CTGTGCCTCC TGCCCTCACC 1320 CCGCTTGGCA CATTTTTGAG ATCTGTATCT ACCCTAAGGT TTGCGCAAAG ACCTCATATG 1380 ACTGCATCTG GCTAAACTGA CAACAGAGGA ATGAAAACAA TCGAGAAACA CATGGTCCTA 1440 GAGAGAAAAT GCAGGGGCTG ACCCCAAGGC TGGGAAGTGA GCATCACCTC TCCACACCAG 1500 TTTCTGTGGC CTCTGGGGAA AAGACAGAAT AAAAACTAGA CTACAGGAGG TGGGGAGGGT 1560 GAACACGTAC AAATCATAGT GAGAAAGAAC CAGTAAGACC TGGTGTTTGC CAGCACAACA 1620 GGATTACAAG CAACAATAAT GTATCATACA TTCTTAAACC ACTATGAGTA TAATTGGATT 1680 GTTGGAACAC AAAGGACAAA TGTTTGAGGG GTGGATACCC CTTTACCCTG ATGCGATTAT 1740 TACACACTGC ATGCCTATAT CAAAATATCT CACGTACCCC ATACCTACAA ACGTATGTAC 1800 CATGTACCCA CAAAAATTAC AAATACAAAA ATACAAAAAA AATTAGTCTA AAAACTAGAC 1860 TCTACACTTA AGGCTGGGCA ATTTCACAAA GCCCTTGAAG GGCAGGAGTC TCTTCCAGGC 1920 TCCAGAGGAA TCCAGAGGAT GAAGCAGGAC GCAAAACGAG GCAGCACGTG AGCAGGGAGA 1980 GGGCACAGAG AGGCCCAGAC CCCTCAGGCC ACAGGGACAC AGCCATGCCC AGAGTCCCTT 2040 CAGACCCCTC CCGTCACCCA CAAGGACCTC ATCACTGTCT CAACCCACCT CAGTCTGTGC 2100 AGGGCTGGCA GGCCAGGAAC TGCAGCCTCC TCCTACCTCC CCCCACCCGG GGTAGCCTGC 2160 AGGAAGACCG GGGAGGGGAG AAGCAGAGAG CAAAGCATGC CGGGGTGACT CACAGAGGTC 2220
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